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Page 1
Changes in allele frequencies of CSF3R and SETBP1 mutations and evidence of clonal evolution in a chronic neutrophilic leukemia patient treated with ruxolitinib.
Nooruddin Z, Miltgen N, Wei Q, Schowinsky J, Pan Z, Tobin J, Purev E, Gutman JA, Robinson W, Pollyea DA. Nooruddin Z, et al. Among authors: robinson w. Haematologica. 2017 May;102(5):e207-e209. doi: 10.3324/haematol.2016.163089. Epub 2017 Feb 16. Haematologica. 2017. PMID: 28209656 Free PMC article. No abstract available.
Clonality of neutrophilia associated with plasma cell neoplasms: report of a SETBP1 mutation and analysis of a single institution series.
Stevens B, Maxson J, Tyner J, Smith CA, Gutman JA, Robinson W, Jordan CT, Lee CK, Swisshelm K, Tobin J, Wei Q, Schowinsky J, Rinella S, Lee HG, Pollyea DA. Stevens B, et al. Among authors: robinson w. Leuk Lymphoma. 2016;57(4):927-34. doi: 10.3109/10428194.2015.1094697. Epub 2015 Oct 27. Leuk Lymphoma. 2016. PMID: 26389776 Free PMC article.
Analysis of Human Leukocyte Antigen DR Alleles, Immune-Related Adverse Events, and Survival Associated With Immune Checkpoint Inhibitor Use Among Patients With Advanced Malignant Melanoma.
Akturk HK, Couts KL, Baschal EE, Karakus KE, Van Gulick RJ, Turner JA, Pyle L, Robinson WA, Michels AW. Akturk HK, et al. Among authors: robinson wa. JAMA Netw Open. 2022 Dec 1;5(12):e2246400. doi: 10.1001/jamanetworkopen.2022.46400. JAMA Netw Open. 2022. PMID: 36512357 Free PMC article.
Expanding the landscape of oncogenic drivers and treatment options in acral and mucosal melanomas by targeted genomic profiling.
Turner JA, Van Gulick RJ, Robinson WA, Mughal T, Tobin RP, MacBeth ML, Holman B, Classon A, Bagby SM, Yacob BW, Hartman SJ, Silverman I, Vorwald VM, Gorden N, Gonzalez R, Gay LM, Ali SM, Benson A, Miller VA, Ross JS, Pitts TM, Rioth MJ, Lewis KD, Medina T, McCarter MD, Gonzalez R, Couts KL. Turner JA, et al. Among authors: robinson wa. Int J Cancer. 2024 Nov 15;155(10):1792-1807. doi: 10.1002/ijc.35087. Epub 2024 Jul 12. Int J Cancer. 2024. PMID: 39001563
SASH1 S519N Variant Links Skin Hyperpigmentation and Premature Hair Graying to Dysfunction of Melanocyte Lineage.
Lambert KA, Clements CM, Mukherjee N, Pacheco TR, Shellman SX, Henen MA, Vögeli B, Goldstein NB, Birlea S, Hintzsche J, Caryotakis G, Tan AC, Zhao R, Norris DA, Robinson WA, Wang Y, VanTreeck JG, Shellman YG. Lambert KA, et al. J Invest Dermatol. 2025 Jan;145(1):144-154.e3. doi: 10.1016/j.jid.2024.04.027. Epub 2024 Jun 6. J Invest Dermatol. 2025. PMID: 38848986 Free PMC article.
2,268 results